| Product NDC: | 57691-112 |
| Proprietary Name: | 06 Moisture Foundation SPF 15 |
| Non Proprietary Name: | Octinoxate and Zinc Oxide |
| Active Ingredient(s): | 3.75; 3.9 mg/.5mL; mg/.5mL & nbsp; Octinoxate and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 57691-112 |
| Labeler Name: | The Body Shop Wake Forest |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090906 |
| Package NDC: | 57691-112-30 |
| Package Description: | 30 mL in 1 BOTTLE, PUMP (57691-112-30) |
| NDC Code | 57691-112-30 |
| Proprietary Name | 06 Moisture Foundation SPF 15 |
| Package Description | 30 mL in 1 BOTTLE, PUMP (57691-112-30) |
| Product NDC | 57691-112 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Zinc Oxide |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090906 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | The Body Shop Wake Forest |
| Substance Name | OCTINOXATE; ZINC OXIDE |
| Strength Number | 3.75; 3.9 |
| Strength Unit | mg/.5mL; mg/.5mL |
| Pharmaceutical Classes |